Substituent and solvent effects on the photo-physical properties of some coumarin dyes

Absorption and fluorescence spectra of three coumarin dyes with various substituents and alkyl groups have been recorded in solvents in the range of 200–730 nm. The photo-physical behavior of dissolved dye depends on the nature of its environment, i.e. the solvatochromic behaviors of coumarin dyes a...

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Published inSpectrochimica acta. Part A, Molecular and biomolecular spectroscopy Vol. 77; no. 2; pp. 337 - 341
Main Authors Zakerhamidi, M.S., Ghanadzadeh, A., Tajalli, H., Moghadam, M., Jassas, M., Hosseini nia, R.
Format Journal Article
LanguageEnglish
Published England Elsevier B.V 01.10.2010
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Abstract Absorption and fluorescence spectra of three coumarin dyes with various substituents and alkyl groups have been recorded in solvents in the range of 200–730 nm. The photo-physical behavior of dissolved dye depends on the nature of its environment, i.e. the solvatochromic behaviors of coumarin dyes and solvent/solute hydrogen bonding interactions can be analyzed by means of linear solvation energy relationships concept proposed by Kamlet and Taft. The intensity, shape, and maximum wavelength of the absorption and fluorescence band of these dyes in solution depend strongly on the solvent–solute interactions and solvent nature. Hydrogen bonding interactions (specific solute–solvent interactions) between these dye–solvent complex and dipolarity/polarizability (non-specific solute–solvent interactions) control reorientation of solvent molecules around the dye.
AbstractList Absorption and fluorescence spectra of three coumarin dyes with various substituents and alkyl groups have been recorded in solvents in the range of 200–730 nm. The photo-physical behavior of dissolved dye depends on the nature of its environment, i.e. the solvatochromic behaviors of coumarin dyes and solvent/solute hydrogen bonding interactions can be analyzed by means of linear solvation energy relationships concept proposed by Kamlet and Taft. The intensity, shape, and maximum wavelength of the absorption and fluorescence band of these dyes in solution depend strongly on the solvent–solute interactions and solvent nature. Hydrogen bonding interactions (specific solute–solvent interactions) between these dye–solvent complex and dipolarity/polarizability (non-specific solute–solvent interactions) control reorientation of solvent molecules around the dye.
Absorption and fluorescence spectra of three coumarin dyes with various substituents and alkyl groups have been recorded in solvents in the range of 200-730 nm. The photo-physical behavior of dissolved dye depends on the nature of its environment, i.e. the solvatochromic behaviors of coumarin dyes and solvent/solute hydrogen bonding interactions can be analyzed by means of linear solvation energy relationships concept proposed by Kamlet and Taft. The intensity, shape, and maximum wavelength of the absorption and fluorescence band of these dyes in solution depend strongly on the solvent-solute interactions and solvent nature. Hydrogen bonding interactions (specific solute-solvent interactions) between these dye-solvent complex and dipolarity/polarizability (non-specific solute-solvent interactions) control reorientation of solvent molecules around the dye.
Author Tajalli, H.
Hosseini nia, R.
Moghadam, M.
Ghanadzadeh, A.
Jassas, M.
Zakerhamidi, M.S.
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Cites_doi 10.1016/j.saa.2007.04.016
10.1016/0584-8539(91)80090-6
10.1039/ft9959102739
10.1021/ja00177a010
10.1016/S0143-7208(01)00018-3
10.1021/jo00165a018
10.1002/ange.19790910206
10.1021/j100074a003
10.1002/9780470171929.ch6
10.1021/ja00418a009
10.1021/ja00467a039
10.1016/0371-1951(64)80185-5
10.1016/0009-2614(92)85364-G
10.1039/P29790000349
10.1016/S0143-7208(99)00012-1
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Issue 2
Keywords Solvent–solute interactions
Solvent polarity scale
Coumarin dyes
Linear solvation energy relationships
Orientation polarizability
Language English
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References Kessler, Wolfbeis (bib11) 1991; 47
Reichardt (bib12) 1979; 91
Reichardt (bib7) 1988
Ravi, Soujanya, Samanta, Radhakrishnan (bib5) 1995; 91
Kamlet, Abboud, Abraham, Taft (bib14) 1983; 48
Kamlet, Abboud, Taft (bib17) 1981; 13
Fox, Rosch (bib9) 1992; 191
Mannekutla, Mulimani, Inamdar (bib6) 2008; 69
Lakowicz (bib21) 2006
Kamlet, Taft (bib20) 1979; 2
Dubois, Goetz, Bienvenue (bib10) 1964; 24
DeBolt, Kollman (bib8) 1990; 112
Kosower (bib13) 1968
Kamlet, Taft (bib19) 1976; 98
Laurence, Nicolet, Dalati, Abboud, Notario (bib22) 1994; 98
Chandrashekharan, Kelly (bib3) 2002; 15
Hirsch (bib15) 1974
Gutmann (bib16) 1978
Abboud, Kamlet, Taft (bib18) 1977; 99
Dall’Acqua, Vedaldi, Caffieri (bib1) 1996
Christie, Lui (bib2) 1999; 42
Sokodowska, Czajkowski, Podsiadly (bib4) 2001; 49
Dall’Acqua (10.1016/j.saa.2009.12.060_bib1) 1996
Kamlet (10.1016/j.saa.2009.12.060_bib17) 1981; 13
Lakowicz (10.1016/j.saa.2009.12.060_bib21) 2006
Mannekutla (10.1016/j.saa.2009.12.060_bib6) 2008; 69
Reichardt (10.1016/j.saa.2009.12.060_bib7) 1988
Fox (10.1016/j.saa.2009.12.060_bib9) 1992; 191
Kosower (10.1016/j.saa.2009.12.060_bib13) 1968
Laurence (10.1016/j.saa.2009.12.060_bib22) 1994; 98
Sokodowska (10.1016/j.saa.2009.12.060_bib4) 2001; 49
Dubois (10.1016/j.saa.2009.12.060_bib10) 1964; 24
Hirsch (10.1016/j.saa.2009.12.060_bib15) 1974
Chandrashekharan (10.1016/j.saa.2009.12.060_bib3) 2002; 15
Kamlet (10.1016/j.saa.2009.12.060_bib20) 1979; 2
Kamlet (10.1016/j.saa.2009.12.060_bib19) 1976; 98
Kamlet (10.1016/j.saa.2009.12.060_bib14) 1983; 48
Kessler (10.1016/j.saa.2009.12.060_bib11) 1991; 47
Gutmann (10.1016/j.saa.2009.12.060_bib16) 1978
Christie (10.1016/j.saa.2009.12.060_bib2) 1999; 42
DeBolt (10.1016/j.saa.2009.12.060_bib8) 1990; 112
Reichardt (10.1016/j.saa.2009.12.060_bib12) 1979; 91
Abboud (10.1016/j.saa.2009.12.060_bib18) 1977; 99
Ravi (10.1016/j.saa.2009.12.060_bib5) 1995; 91
References_xml – volume: 98
  start-page: 5807
  year: 1994
  ident: bib22
  publication-title: J. Phys. Chem.
  contributor:
    fullname: Notario
– volume: 91
  start-page: 2739
  year: 1995
  ident: bib5
  publication-title: J. Chem. Soc., Faraday Trans.
  contributor:
    fullname: Radhakrishnan
– volume: 13
  start-page: 485
  year: 1981
  ident: bib17
  publication-title: Prog. Phys. Org. Chem.
  contributor:
    fullname: Taft
– year: 1978
  ident: bib16
  article-title: The Donor–Acceptor Approach to Molecular Interactions
  contributor:
    fullname: Gutmann
– volume: 99
  start-page: 8325
  year: 1977
  ident: bib18
  publication-title: J. Am. Chem. Soc.
  contributor:
    fullname: Taft
– volume: 112
  start-page: 7515
  year: 1990
  ident: bib8
  publication-title: J. Am. Chem. Soc.
  contributor:
    fullname: Kollman
– volume: 48
  start-page: 2877
  year: 1983
  ident: bib14
  publication-title: J. Org. Chem.
  contributor:
    fullname: Taft
– year: 2006
  ident: bib21
  article-title: Principles of Fluorescence Spectroscopy
  contributor:
    fullname: Lakowicz
– volume: 24
  start-page: 1815
  year: 1964
  ident: bib10
  publication-title: Spectrochim. Acta A
  contributor:
    fullname: Bienvenue
– volume: 15
  start-page: 1
  year: 2002
  ident: bib3
  publication-title: Spectrum
  contributor:
    fullname: Kelly
– volume: 49
  start-page: 187
  year: 2001
  ident: bib4
  publication-title: Dyes Pigm.
  contributor:
    fullname: Podsiadly
– year: 1968
  ident: bib13
  article-title: An Introduction to Physical Organic Chemistry
  contributor:
    fullname: Kosower
– volume: 42
  start-page: 85
  year: 1999
  ident: bib2
  publication-title: Dyes Pigm.
  contributor:
    fullname: Lui
– year: 1988
  ident: bib7
  article-title: Solvents and Solvent Effects in Organic Chemistry
  contributor:
    fullname: Reichardt
– volume: 91
  start-page: 119
  year: 1979
  ident: bib12
  publication-title: Angew. Chem.
  contributor:
    fullname: Reichardt
– volume: 98
  start-page: 377
  year: 1976
  ident: bib19
  publication-title: J. Am. Chem. Soc.
  contributor:
    fullname: Taft
– volume: 69
  start-page: 419
  year: 2008
  ident: bib6
  publication-title: Spectrochim. Acta A
  contributor:
    fullname: Inamdar
– start-page: 1
  year: 1996
  end-page: 16
  ident: bib1
  publication-title: The Fundamental Bases of Phototherapy
  contributor:
    fullname: Caffieri
– volume: 47
  start-page: 187
  year: 1991
  ident: bib11
  publication-title: Spectrochim. Acta A
  contributor:
    fullname: Wolfbeis
– volume: 2
  start-page: 349
  year: 1979
  ident: bib20
  publication-title: J. Chem. Soc., Perkin Trans.
  contributor:
    fullname: Taft
– year: 1974
  ident: bib15
  article-title: Concepts in Theoretical Organic Chemistry
  contributor:
    fullname: Hirsch
– volume: 191
  start-page: 33
  year: 1992
  ident: bib9
  publication-title: Chem. Phys. Lett.
  contributor:
    fullname: Rosch
– volume: 69
  start-page: 419
  year: 2008
  ident: 10.1016/j.saa.2009.12.060_bib6
  publication-title: Spectrochim. Acta A
  doi: 10.1016/j.saa.2007.04.016
  contributor:
    fullname: Mannekutla
– volume: 47
  start-page: 187
  year: 1991
  ident: 10.1016/j.saa.2009.12.060_bib11
  publication-title: Spectrochim. Acta A
  doi: 10.1016/0584-8539(91)80090-6
  contributor:
    fullname: Kessler
– volume: 91
  start-page: 2739
  year: 1995
  ident: 10.1016/j.saa.2009.12.060_bib5
  publication-title: J. Chem. Soc., Faraday Trans.
  doi: 10.1039/ft9959102739
  contributor:
    fullname: Ravi
– volume: 112
  start-page: 7515
  year: 1990
  ident: 10.1016/j.saa.2009.12.060_bib8
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja00177a010
  contributor:
    fullname: DeBolt
– volume: 49
  start-page: 187
  year: 2001
  ident: 10.1016/j.saa.2009.12.060_bib4
  publication-title: Dyes Pigm.
  doi: 10.1016/S0143-7208(01)00018-3
  contributor:
    fullname: Sokodowska
– volume: 48
  start-page: 2877
  year: 1983
  ident: 10.1016/j.saa.2009.12.060_bib14
  publication-title: J. Org. Chem.
  doi: 10.1021/jo00165a018
  contributor:
    fullname: Kamlet
– year: 2006
  ident: 10.1016/j.saa.2009.12.060_bib21
  contributor:
    fullname: Lakowicz
– year: 1988
  ident: 10.1016/j.saa.2009.12.060_bib7
  contributor:
    fullname: Reichardt
– volume: 91
  start-page: 119
  year: 1979
  ident: 10.1016/j.saa.2009.12.060_bib12
  publication-title: Angew. Chem.
  doi: 10.1002/ange.19790910206
  contributor:
    fullname: Reichardt
– year: 1968
  ident: 10.1016/j.saa.2009.12.060_bib13
  contributor:
    fullname: Kosower
– volume: 98
  start-page: 5807
  year: 1994
  ident: 10.1016/j.saa.2009.12.060_bib22
  publication-title: J. Phys. Chem.
  doi: 10.1021/j100074a003
  contributor:
    fullname: Laurence
– start-page: 1
  year: 1996
  ident: 10.1016/j.saa.2009.12.060_bib1
  contributor:
    fullname: Dall’Acqua
– volume: 13
  start-page: 485
  year: 1981
  ident: 10.1016/j.saa.2009.12.060_bib17
  publication-title: Prog. Phys. Org. Chem.
  doi: 10.1002/9780470171929.ch6
  contributor:
    fullname: Kamlet
– year: 1978
  ident: 10.1016/j.saa.2009.12.060_bib16
  contributor:
    fullname: Gutmann
– volume: 98
  start-page: 377
  year: 1976
  ident: 10.1016/j.saa.2009.12.060_bib19
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja00418a009
  contributor:
    fullname: Kamlet
– volume: 99
  start-page: 8325
  year: 1977
  ident: 10.1016/j.saa.2009.12.060_bib18
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja00467a039
  contributor:
    fullname: Abboud
– volume: 24
  start-page: 1815
  year: 1964
  ident: 10.1016/j.saa.2009.12.060_bib10
  publication-title: Spectrochim. Acta A
  doi: 10.1016/0371-1951(64)80185-5
  contributor:
    fullname: Dubois
– volume: 191
  start-page: 33
  year: 1992
  ident: 10.1016/j.saa.2009.12.060_bib9
  publication-title: Chem. Phys. Lett.
  doi: 10.1016/0009-2614(92)85364-G
  contributor:
    fullname: Fox
– volume: 15
  start-page: 1
  year: 2002
  ident: 10.1016/j.saa.2009.12.060_bib3
  publication-title: Spectrum
  contributor:
    fullname: Chandrashekharan
– year: 1974
  ident: 10.1016/j.saa.2009.12.060_bib15
  contributor:
    fullname: Hirsch
– volume: 2
  start-page: 349
  year: 1979
  ident: 10.1016/j.saa.2009.12.060_bib20
  publication-title: J. Chem. Soc., Perkin Trans.
  doi: 10.1039/P29790000349
  contributor:
    fullname: Kamlet
– volume: 42
  start-page: 85
  year: 1999
  ident: 10.1016/j.saa.2009.12.060_bib2
  publication-title: Dyes Pigm.
  doi: 10.1016/S0143-7208(99)00012-1
  contributor:
    fullname: Christie
SSID ssj0001820
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Snippet Absorption and fluorescence spectra of three coumarin dyes with various substituents and alkyl groups have been recorded in solvents in the range of 200–730...
Absorption and fluorescence spectra of three coumarin dyes with various substituents and alkyl groups have been recorded in solvents in the range of 200-730...
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elsevier
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StartPage 337
SubjectTerms Absorption
Coloring Agents - chemistry
Coumarin dyes
Coumarins - chemistry
Hydrogen Bonding
Indicators and Reagents - chemistry
Light
Linear solvation energy relationships
Molecular Structure
Orientation polarizability
Solvent polarity scale
Solvents - chemistry
Solvent–solute interactions
Spectrometry, Fluorescence
Title Substituent and solvent effects on the photo-physical properties of some coumarin dyes
URI https://dx.doi.org/10.1016/j.saa.2009.12.060
https://www.ncbi.nlm.nih.gov/pubmed/20609617
Volume 77
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